IP Library Granted Patent US 9,650,352
Granted Patent B2
US 9,650,352 · App. 14/351,441 · Granted May 16, 2017

Use of (2R, 6R)-hydroxynorketamine, (S)-dehydronorketamine and other stereoisomeric dehydro and hydroxylated metabolites of (R,S)-ketamine in the treatment of depression and neuropathic pain

Inventors: Irving W. Wainer (Washington, DC); Ruin Moaddel (Bel Air, MD); Michel Bernier (Pikesville, MD); Carlos A. Zarate (Germantown, MD); Marc C. Torjman (Southampton, PA); Michael E. Goldberg (Philadelphia, PA); Mary J. Tanga (Los Altos, CA)
Assignees: THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES; COOPER HEALTH SYSTEM; SRI INTERNATIONAL
C07D295/155C07C225/20C07C229/48C07C237/04C07C237/20C07D295/108C07D295/112C07D295/15C07B2200/07C07C2101/14C07C2101/16
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Quick Facts
Patent No.
US 9,650,352
App. No.
14/351,441
Granted
May 16, 2017
Kind
B2
Abstract

The disclosure provides pharmaceutical preparations containing (2R,6R)-hydroxynorketamine, or (R)- or (S)-dehydronorketamine, or other stereoisomeric dehydro or hydroxylated ketamine metabolite. (2R,6R)-hydroxynorketamine The disclosure also provides novel ketamine metabolite prodrugs. The disclosure provides methods of treating, bipolar depression, major depressive disorder, neuropathic and chronic pain, including complex regional pain disorder (CRPS) by administering a purified ketamine metabolite or a ketamine metabolite prodrug directly to patients in need of such treatment.

Claims (48)

1. A compound of the formula

or a pharmaceutically acceptable salt thereof, wherein

R 1 is hydroxyl or -A 1 B 1 where A 1 is —O—, —O(C═O)—, —(C═O)O—, —O(C═O)O—, —O(C═O)NR 6 —, —OS(O) 2 —, —OS(O) 3 , or —OP(O) 3 —, and B 1 is C 1 -C 8 alkyl, C 2 -C 8 alkenyl, C 2 -C 8 alkynyl, (carbocycle)C 0 -C 4 alkyl or (heterocycle)C 0 -C 4 alkyl, each of which is substituted with from 0 to 4 substituents independently chosen from halogen, hydroxyl, amino, cyano, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 1 -C 6 alkylester, mono- and di-(C 1 -C 4 alkyl)amino, (C 3 -C 7 cycloalkyl)C 0 -C 2 alkyl, (heterocycloalkyl)C 0 -C 2 alkyl, C 1 -C 2 haloalkyl, and C 1 -C 2 haloalkoxy; with the proviso that -A 1 B 1 is not (4-methylphenyl)-S(O) 2 O—;

wherein the six-membered ring to which R 1 is bound is fully saturated when R 1 is hydroxyl or -A 1 B 1 ;

R 2 is hydrogen or -A 2 B 2 where A 2 is a bond, —O(C═O)—, —(C═O)O—, —S(O) 2 —, —(S═O)NR 6 —, or —(C═O)NR 6 —, B 2 is C 1 -C 8 alkyl, C 2 -C 8 alkenyl, C 2 -C 8 alkynyl, C 2 -C 6 alkanoyl, (carbocycle)C 0 -C 4 alkyl, (heterocycle)C 0 -C 4 alkyl, or an amino acid or dipeptide covalently bound to A 2 by its C-terminus, each of which is substituted with from 0 to 4 substituents independently chosen from halogen, hydroxyl, amino, cyano, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 1 -C 6 alkylester, mono- and di-(C 1 -C 4 alkyl)amino, (C 3 -C 7 cycloalkyl)C 0 -C 2 alkyl, (heterocycloalkyl)C 0 -C 2 alkyl, C 1 -C 2 haloalkyl, and C 1 -C 2 haloalkoxy; with the proviso that B 2 is not methyl when A 2 is a bond or —(C═O)O—;

R 1 is not hydroxyl when R 2 is hydrogen;

R 3 is hydrogen;

R 4 and R 5 are 0 or 1 or more substituents independently chosen from halogen, hydroxyl, amino, cyano, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, mono- and di-C 1 -C 4 alkylamino, C 1 -C 2 haloalkyl, and C 1 -C 2 haloalkoxy; and

R 6 is hydrogen or C 1 -C 6 alkyl.

2. A compound or salt of claim 1 , of the formula

3. A compound of the formula

or a pharmaceutically acceptable salt thereof,

where A 1 is —O—, —O(C═O)—, or —O(C═O)O—and B 1 is C 1 -C 8 alkyl, C 2 -C 8 alkenyl, C 2 -C 8 alkynyl, (carbocycle)C 0 -C 4 alkyl or (heterocycle)C 0 -C 4 alkyl, each of which is substituted with from 0 to 4 substituents independently chosen from halogen, hydroxyl, amino, cyano, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 1 -C 6 alkylester, mono- and di-(C 1 -C 4 alkyl)amino, (C 3 -C 7 cycloalkyl)C 0 -C 2 alkyl, (heterocycloalkyl)C 0 -C 2 alkyl, C 1 -C 2 haloalkyl, and C 1 -C 2 haloalkoxy;

R 2 is hydrogen or -A 2 B 2 where A 2 is a bond, —O(C═O)—, —(C═O)O—, —S(O) 2 —, —(S═O)NR 6 —, or —(C═O)NR 6 —, B 2 is C 1 -C 8 alkyl, C 2 -C 8 alkenyl, C 2 -C 8 alkynyl, C 2 -C 6 alkanoyl, (carbocycle)C 0 -C 4 alkyl, (heterocycle)C 0 -C 4 alkyl, or an amino acid or dipeptide covalently bound to A 2 by its C-terminus, each of which is substituted with from 0 to 4 substituents independently chosen from halogen, hydroxyl, amino, cyano, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 1 -C 6 alkylester, mono- and di-(C 1 -C 4 alkyl)amino, (C 3 -C 7 cycloalkyl)C 0 -C 2 alkyl, (heterocycloalkyl)C 0 -C 2 alkyl, C 1 -C 2 haloalkyl, and C 1 -C 2 haloalkoxy; with the proviso that B 2 is not methyl when A 2 is a bond or —(C═O)O—;

R 3 is hydrogen or C 1 -C 6 alkyl;

R 4 and R 5 are 0 or 1 or more substituents independently chosen from halogen, hydroxyl, amino, cyano, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, mono- and di-C 1 -C 4 alkylamino, C 1 -C 2 haloalkyl, and C 1 -C 2 haloalkoxy; and

R 6 is hydrogen or C 1 -C 6 alkyl.

4. A compound or salt of claim 3 , wherein

R 3 is hydrogen;

R 4 and R 5 are each 0 to 2 substituents independently chosen from halogen, hydroxyl, amino, C 1 -C 2 alkyl, and C 1 -C 2 alkyl; and

R 6 is hydrogen or methyl.

5. A compound or salt of claim 4 , wherein

R 2 is -A 2 B 2 where A 2 is a bond, —(C═O)O—, —S(O) 2 —, —(S═O)NR 6 —, or —(C═O)NR 6 —, B 2 is C 1 -C 6 alkyl, C 2 -C 4 alkanoyl, (phenyl)C 0 -C 2 alkyl, (C 3 -C 7 cycloalkyl)C 0 -C 4 alkyl, (heterocycloalkyl)C 0 -C 2 alkyl, (5- or 6-membered heteroaryl)C 0 -C 2 alkyl, or an amino acid covalently bound to A 2 by its C-terminus, each of which is substituted with from 0 to 4 substituents independently chosen from halogen, hydroxyl, amino, cyano, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 1 -C 6 alkylester, mono- and di-(C 1 -C 4 alkyl)amino, C 1 -C 2 haloalkyl, and C 1 -C 2 haloalkoxy.

6. A compound or salt of claim 4 , where

A 2 is a bond or —(C═O)O— and B 2 is C 2 -C 6 alkyl, (phenyl)C 0 -C 2 alkyl, or (C 3 -C 7 alkyl)C 0 -C 4 alkyl, each of which is substituted with from 0 to 4 substituents independently chosen from halogen, hydroxyl, amino, cyano, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, and mono- and di-(C 1 -C 4 alkyl)amino.

7. A compound of the formula

or a pharmaceutically acceptable salt thereof, wherein:

R 1 is -A 1 B 1 where A 1 is —O—, —O(C═O)—, —(C═O)O—, —O(C═O)O—, —O(C═O)NR 6 —, —OS(O) 2 —, —OS(O) 3 , or —OP(O) 3 —, and B 1 is C 1 -C 8 alkyl, C 2 -C 8 alkenyl, C 2 -C 8 alkynyl, (carbocycle)C 0 -C 4 alkyl or (heterocycle)C 0 -C 4 alkyl, each of which is substituted with from 0 to 4 substituents independently chosen from halogen, hydroxyl, amino, cyano, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 1 -C 6 alkylester, mono- and di-(C 1 -C 4 alkyl)amino, (C 3 -C 7 cycloalkyl)C 0 -C 2 alkyl, (heterocycloalkyl)C 0 -C 2 alkyl, C 1 -C 2 haloalkyl, and C 1 -C 2 haloalkoxy; with the proviso that -A 1 B 1 is not (4-methylphenyl)-S(O) 2 O—;

R 2 is hydrogen;

R 3 is hydrogen;

R 4 and R 5 are each 0 to 2 substituents independently chosen from halogen, hydroxyl, amino, C 1 -C 2 alkyl, and C 1 -C 2 alkyl; and

R 6 is hydrogen or methyl.

8. A compound or salt of claim 7 , where

R 1 is -A 1 B 1 where A 1 is —O(C═O)— or —O(C═O)O—, and B 1 is C 1 -C 6 alkyl, (phenyl)C 0 -C 4 alkyl, (C 3 -C 7 cycloalkyl)C 0 -C 4 alkyl, (heterocycloalkyl)C 0 -C 2 alkyl, or (5- or 6-membered heteroaryl)C 0 -C 2 alkyl, each of which is substituted with from 0 to 4 substituents independently chosen from halogen, hydroxyl, amino, cyano, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 1 -C 6 alkylester, mono- and di-(C 1 -C 4 alkyl)amino, (C 3 -C 7 cycloalkyl)C 0 -C 2 alkyl, (heterocycloalkyl)C 0 -C 2 alkyl, C 1 -C 2 haloalkyl, and C 1 -C 2 haloalkoxy.

9. A method of treating bipolar depression, major depressive disorder, schizophrenia, Alzheimer's dementia, amyotrophic lateral sclerosis, complex regional pain syndrome (CRPS), chronic pain, or neuropathic pain comprising administering an effective amount of a compound or salt of claim 1 , to a patient in need of such treatment.

10. The method of claim 9 , wherein an effective amount is an amount effective to decrease painful symptoms; wherein a decrease in painful symptom is the achievement of a 50% or greater reduction of painful symptoms on a pain rating scale.

11. A pharmaceutical composition comprising a compound or salt of claim 1 , together with a pharmaceutically acceptable carrier.

12. The pharmaceutical composition of claim 11 , wherein the composition is a solution and contains from about 0.05 mg/ml to about 0.5 mg/ml.

13. A compound or salt of claim 8 , of the formula

14. The pharmaceutical composition of claim 11 , wherein the composition is formulated for oral administration, intravenous administration, or intramuscular injection.

15. A method of treating bipolar depression, major depressive disorder, schizophrenia, Alzheimer's dementia, amyotrophic lateral sclerosis, complex regional pain syndrome (CRPS), chronic pain, or neuropathic pain comprising administering an effective amount of a compound or salt of claim 3 , to a patient in need of such treatment.

16. A pharmaceutical composition comprising a compound or salt of claim 3 , together with a pharmaceutically acceptable carrier.

17. The pharmaceutical composition of claim 3 , wherein the composition is formulated for oral administration, intravenous administration, or intramuscular injection.

18. The pharmaceutical composition of claim 3 , wherein the composition is a solution and contains from about 0.05 mg/ml to about 0.5 mg/ml.

19. A method of treating bipolar depression, major depressive disorder, schizophrenia, Alzheimer's dementia, amyotrophic lateral sclerosis, complex regional pain syndrome (CRPS), chronic pain, or neuropathic pain comprising administering an effective amount of a compound or salt of claim 7 , to a patient in need of such treatment.

20. A pharmaceutical composition comprising a compound or salt of claim 7 , together with a pharmaceutically acceptable excipient.

21. The pharmaceutical composition of claim 7 , wherein the composition is formulated for oral administration, intravenous administration, or intramuscular injection.

22. The pharmaceutical composition of claim 7 , wherein the composition is a solution and contains from about 0.05 mg/ml to about 0.5 mg/ml.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 23, 2015
From: TANGA, MARY J.
To: SRI INTERNATIONAL
Reel/Frame 035227/0992 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 23, 2015
From: TORJMAN, MARC C.; GOLDBERG, MICHAEL E.
To: COOPER HEALTH SYSTEM
Reel/Frame 035228/0014 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 23, 2015
From: WAINER, IRVING W.; MOADDEL, RUIN; BERNIER, MICHEL; ZARATE, CARLOS A.
To: THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES
Reel/Frame 035228/0033 →
Continuity (2)
Provisional Application 61547336 · Oct 14, 2011
Related Publication 20140296241A1 · Oct 2, 2014